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wtap monoclonal antibody  (Proteintech)


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    Structured Review

    Proteintech wtap monoclonal antibody
    Wtap Monoclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 228 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/wtap+monoclonal+antibody/WTAP+Antibody/pmc12834426-37-36-40
    Average 96 stars, based on 228 article reviews
    wtap monoclonal antibody - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Western Blot:

    Article Title: Systematic assessment of transcriptomic and metabolic reprogramming by blue light exposure coupled with aging.
    Article Snippet: .. The primary antibodies used for Western blotting included a β-Actin Mouse Monoclonal Antibody (#AF5001, Beyotime Biotech Co., Ltd.), METTL3 Polyclonal antibody (#15073-1-AP, Proteintech, USA), METTL14 Polyclonal antibody (#HPA038002, Sigma, USA), WTAP Monoclonal antibody (#60188-1-Ig, Proteintech), Recombinant Anti-mTOR antibody [EPR390(N)] (#ab134903, Abcam, England), and Recombinant Anti-PER3 antibody (EPR13038) (#ab177482, Abcam, USA). .. After incubation with the corresponding secondary antibody, each targeted protein was detected using Clarity Western ECL Substrate (#1705060, Bio-Rad, Hercules, CA, USA) and photographed with a Tanon 5200 Chemiluminescent Imaging System (Tanon, Shanghai, China).

    Article Title: Systematic assessment of transcriptomic and metabolic reprogramming by blue light exposure coupled with aging
    Article Snippet: .. The primary antibodies used for Western blotting included a β-Actin Mouse Monoclonal Antibody (#AF5001, Beyotime Biotech Co., Ltd.), METTL3 Polyclonal antibody (#15073-1-AP, Proteintech, USA), METTL14 Polyclonal antibody (#HPA038002, Sigma, USA), WTAP Monoclonal antibody (#60188-1-Ig, Proteintech), Recombinant Anti-mTOR antibody [EPR390(N)] (#ab134903, Abcam, England), and Recombinant Anti-PER3 antibody (EPR13038) (#ab177482, Abcam, USA). .. After incubation with the corresponding secondary antibody, each targeted protein was detected using Clarity Western ECL Substrate (#1705060, Bio-Rad, Hercules, CA, USA) and photographed with a Tanon 5200 Chemiluminescent Imaging System (Tanon, Shanghai, China).

    Recombinant:

    Article Title: Systematic assessment of transcriptomic and metabolic reprogramming by blue light exposure coupled with aging.
    Article Snippet: .. The primary antibodies used for Western blotting included a β-Actin Mouse Monoclonal Antibody (#AF5001, Beyotime Biotech Co., Ltd.), METTL3 Polyclonal antibody (#15073-1-AP, Proteintech, USA), METTL14 Polyclonal antibody (#HPA038002, Sigma, USA), WTAP Monoclonal antibody (#60188-1-Ig, Proteintech), Recombinant Anti-mTOR antibody [EPR390(N)] (#ab134903, Abcam, England), and Recombinant Anti-PER3 antibody (EPR13038) (#ab177482, Abcam, USA). .. After incubation with the corresponding secondary antibody, each targeted protein was detected using Clarity Western ECL Substrate (#1705060, Bio-Rad, Hercules, CA, USA) and photographed with a Tanon 5200 Chemiluminescent Imaging System (Tanon, Shanghai, China).

    Article Title: Systematic assessment of transcriptomic and metabolic reprogramming by blue light exposure coupled with aging
    Article Snippet: .. The primary antibodies used for Western blotting included a β-Actin Mouse Monoclonal Antibody (#AF5001, Beyotime Biotech Co., Ltd.), METTL3 Polyclonal antibody (#15073-1-AP, Proteintech, USA), METTL14 Polyclonal antibody (#HPA038002, Sigma, USA), WTAP Monoclonal antibody (#60188-1-Ig, Proteintech), Recombinant Anti-mTOR antibody [EPR390(N)] (#ab134903, Abcam, England), and Recombinant Anti-PER3 antibody (EPR13038) (#ab177482, Abcam, USA). .. After incubation with the corresponding secondary antibody, each targeted protein was detected using Clarity Western ECL Substrate (#1705060, Bio-Rad, Hercules, CA, USA) and photographed with a Tanon 5200 Chemiluminescent Imaging System (Tanon, Shanghai, China).

    other:

    Article Title: The Flip Side of the Coin: METTL3 Serves as a Novel Cellular Senescence Accelerator via Negative Regulation of ITGA9
    Article Snippet: M6A antibody (202003, Synaptic Systems, Germany), GAPDH Monoclonal antibody (60004-1-Ig, Proteintech, China), METTL3 Monoclonal antibody (ab195352, Abcam, UK), FTO Polyclonal antibody (27226-1-AP, Proteintech, China), METTL14 Polyclonal antibody (AP22363a, Abgent, USA), ALKBH5 Polyclonal antibody (16837-1-AP, Proteintech, China), WTAP Monoclonal antibody (60188-1-Ig, Proteintech, China), p16 INK4A antibody (F-12) (sc-1661, Santa Cruz, USA), ITGA9 Polyclonal antibody (AF3827, R&D, USA), BrdU Monoclonal antibody (66241-1-Ig, Proteintech, China), Goat Anti-Mouse antibody (Alexa Fluor® 488) (SA00013-1, Proteintech, China), Goat anti-rabbit IgG (H+L) antibody (A0208, Beyotime, China), Goat anti-mouse IgG (H+L) antibody (A0216, Beyotime, China), Donkey anti-goat IgG (H+L) antibody (A0181, Beyotime, China).



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    Figure 2. The Expression of m6A “Writers” in EGFR Wild Type and EGFR Mutated NSLCL Tissues. (A) Typical Pictures of Immunohistochemical Staining of m6A “Writers” in EGFR-w.t. and EGFR-Mut. NSCLC Tissues. The Scale Bar in the Images Represents 100 μm and 20 μm Respectively. Images Were Collected at a 40× Objective Magnification (Numerical Aperture 0.75) Using an M8 Digital Microscope. (B) Immunohistochemical Staining Index of METTLE3 in EGFR-Mut. Tissues Compared With EGFR-w.t. (w.t., n = 103; EGFR- Mut., n = 143). (C) Immunohistochemical Staining Index of METTLE14 in EGFR-Mut. Tissues Compared With EGFR-w.t. (w.t., n = 103; EGFR-Mut., n = 143). (D) Immunohistochemical Staining Index <t>of</t> <t>RBM15</t> in EGFR-Mut. Tissues Compared With EGFR-w.t. (w.t., n = 103; EGFR-Mut., n = 143). (E) Immunohistochemical Staining Index of <t>WTAP</t> in EGFR-Mut. Tissues Compared With EGFR-w.t. (w.t., n = 103; EGFR-Mut., n = 143). Each bar Represents the Median Values ± Quartile Values. P Value was Determined by Unpaired t Test.
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    Figure 2. The Expression of m6A “Writers” in EGFR Wild Type and EGFR Mutated NSLCL Tissues. (A) Typical Pictures of Immunohistochemical Staining of m6A “Writers” in EGFR-w.t. and EGFR-Mut. NSCLC Tissues. The Scale Bar in the Images Represents 100 μm and 20 μm Respectively. Images Were Collected at a 40× Objective Magnification (Numerical Aperture 0.75) Using an M8 Digital Microscope. (B) Immunohistochemical Staining Index of METTLE3 in EGFR-Mut. Tissues Compared With EGFR-w.t. (w.t., n = 103; EGFR- Mut., n = 143). (C) Immunohistochemical Staining Index of METTLE14 in EGFR-Mut. Tissues Compared With EGFR-w.t. (w.t., n = 103; EGFR-Mut., n = 143). (D) Immunohistochemical Staining Index <t>of</t> <t>RBM15</t> in EGFR-Mut. Tissues Compared With EGFR-w.t. (w.t., n = 103; EGFR-Mut., n = 143). (E) Immunohistochemical Staining Index of <t>WTAP</t> in EGFR-Mut. Tissues Compared With EGFR-w.t. (w.t., n = 103; EGFR-Mut., n = 143). Each bar Represents the Median Values ± Quartile Values. P Value was Determined by Unpaired t Test.
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    Image Search Results


    Figure 2. The Expression of m6A “Writers” in EGFR Wild Type and EGFR Mutated NSLCL Tissues. (A) Typical Pictures of Immunohistochemical Staining of m6A “Writers” in EGFR-w.t. and EGFR-Mut. NSCLC Tissues. The Scale Bar in the Images Represents 100 μm and 20 μm Respectively. Images Were Collected at a 40× Objective Magnification (Numerical Aperture 0.75) Using an M8 Digital Microscope. (B) Immunohistochemical Staining Index of METTLE3 in EGFR-Mut. Tissues Compared With EGFR-w.t. (w.t., n = 103; EGFR- Mut., n = 143). (C) Immunohistochemical Staining Index of METTLE14 in EGFR-Mut. Tissues Compared With EGFR-w.t. (w.t., n = 103; EGFR-Mut., n = 143). (D) Immunohistochemical Staining Index of RBM15 in EGFR-Mut. Tissues Compared With EGFR-w.t. (w.t., n = 103; EGFR-Mut., n = 143). (E) Immunohistochemical Staining Index of WTAP in EGFR-Mut. Tissues Compared With EGFR-w.t. (w.t., n = 103; EGFR-Mut., n = 143). Each bar Represents the Median Values ± Quartile Values. P Value was Determined by Unpaired t Test.

    Journal: Cancer control : journal of the Moffitt Cancer Center

    Article Title: M6A Methylation Regulators METTL3 and ALKBH5 are Risk Factors for EGFR-Mutant NSCLC.

    doi: 10.1177/10732748251342685

    Figure Lengend Snippet: Figure 2. The Expression of m6A “Writers” in EGFR Wild Type and EGFR Mutated NSLCL Tissues. (A) Typical Pictures of Immunohistochemical Staining of m6A “Writers” in EGFR-w.t. and EGFR-Mut. NSCLC Tissues. The Scale Bar in the Images Represents 100 μm and 20 μm Respectively. Images Were Collected at a 40× Objective Magnification (Numerical Aperture 0.75) Using an M8 Digital Microscope. (B) Immunohistochemical Staining Index of METTLE3 in EGFR-Mut. Tissues Compared With EGFR-w.t. (w.t., n = 103; EGFR- Mut., n = 143). (C) Immunohistochemical Staining Index of METTLE14 in EGFR-Mut. Tissues Compared With EGFR-w.t. (w.t., n = 103; EGFR-Mut., n = 143). (D) Immunohistochemical Staining Index of RBM15 in EGFR-Mut. Tissues Compared With EGFR-w.t. (w.t., n = 103; EGFR-Mut., n = 143). (E) Immunohistochemical Staining Index of WTAP in EGFR-Mut. Tissues Compared With EGFR-w.t. (w.t., n = 103; EGFR-Mut., n = 143). Each bar Represents the Median Values ± Quartile Values. P Value was Determined by Unpaired t Test.

    Article Snippet: The primary antibodies were diluted in antibody diluent (Abcam, Cambridge, MA, USA) with different concentrations of 1:400 ALKBH5 Rab mAb (ab195377, Abcam), 1:200 P53 Mou mAb (DO-7, ZSGB-BIO), 1:200 METTL3 Rab mAb (ab195352, Abcam), 1:100 RBM15 Mou mAb (66059-1-Ig, Proteintech), 1:100 METTL14 Mou mAb (MA5-24706, Thermo-Fisher), 1:200 WTAP Mou mAb (60188-1-Ig, Proteintech), 1:100 FTO Mou mAb (MA527142, Thermo-Fisher), 1:200 YTHDC1 Rab mAb (ab220159, Abcam), 1:400 YTHDC2 Rab poly (PA5-57920, Thermo-Fisher), 1:400 YTHDF1 Rab poly (17479-1-AP, Proteintech), 1:400 YTHDF2 Rab poly (24744-1-AP, Proteintech), and 1:200 YTHDF3 Rab poly (PA5-26983, ThermoFisher).

    Techniques: Expressing, Immunohistochemical staining, Staining, Microscopy